Absorbent structure containing individualized, polycarboxylic acid crosslinked wood pulp cellulose fibers

ABSTRACT

Disclosed are absorbent structures containing individualized, crosslinked fibers. The individualized, crosslinked fibers preferably have a C 2  -C 9  polycarboxylic acid crosslinking agent reacted with the fibers in the form of intrafiber crosslink bonds. Preferably, the crosslinking agent is citric acid, and between about 0.5 mole % and about 10.0 mole % crosslinking agent react to form the intrafiber crosslink bonds. Also preferably, the absorbent structures have actual dry densities greater than their corresponding equilibrium wet densities, and expand upon wetting. The absorbent structures may also contain hydrogel-forming material.

This application is a continuation-in-part of Ser. No. 07/432,705 filedNov. 7, 1989 and since abandoned.

FIELD OF INVENTION

This invention is concerned with cellulosic fibers having high fluidabsorption properties, and especially with absorbent structures madefrom such cellulosic fibers. More specifically, this invention isconcerned with absorbent structures containing individualized,crosslinked, cellulosic fibers.

BACKGROUND OF THE INVENTION

Fibers crosslinked in substantially individualized form and variousmethods for making such fibers have been described in the art. The term"individualized, crosslinked fibers", refers to cellulosic fibers thathave primarily intrafiber chemical crosslink bonds. That is, thecrosslink bonds are primarily between cellulose molecules of a singlefiber, rather than between cellulose molecules of separate fibers.Individualized, crosslinked fibers are generally regarded as beinguseful in absorbent product applications. The fibers themselves andabsorbent structures containing individualized, crosslinked fibersgenerally exhibit an improvement in at least one significant absorbencyproperty relative to conventional, uncrosslinked fibers. Often, theimprovement in absorbency is reported in terms of absorbent capacity.Additionally, absorbent structures made from individualized crosslinkedfibers generally exhibit increased wet resilience and increased dryresilience relative to absorbent structures made from uncrosslinkedfibers. The term "resilience" shall hereinafter refer to the ability ofpads made from cellulosic fibers to return toward an expanded originalstate upon release of a compressional force. Dry resilience specificallyrefers to the ability of an absorbent structure to expand upon releaseof compressional force applied while the fibers are in a substantiallydry condition. Wet resilience specifically refers to the ability of anabsorbent structure to expand upon release of compressional forceapplied while the fibers are in a moistened condition. For the purposesof this invention and consistency of disclosure, wet resilience shall beobserved and reported for an absorbent structure moistened tosaturation.

In general, three categories of processes have been reported for makingindividualized, crosslinked fibers. These processes, described below,are herein referred to as dry crosslinking processes, aqueous solutioncrosslinking processes, and substantially non-aqueous solutioncrosslinking processes.

Processes for making individualized, crosslinked fibers with drycrosslinking technology are described in U.S. Pat. No. 3,224,926, L. J.Bernardin, issued Dec. 21, 1965. Individualized, crosslinked fibers areproduced by impregnating swollen fibers in an aqueous solution withcrosslinking agent, dewatering and defiberizing the fibers by mechanicalaction, and drying the fibers at elevated temperature to effectcrosslinking while the fibers are in a substantially individual state.The fibers are inherently crosslinked in an unswollen, collapsed stateas a result of being dehydrated prior to crosslinking. Processes asexemplified in U.S. Pat. Nos. 3,224,926, wherein crosslinking is causedto occur while the fibers are in an unswollen, collapsed state, arereferred to as processes for making "dry crosslinked" fibers. Drycrosslinked fibers are generally highly stiffened by crosslink bonds,and absorbent structures made therefrom exhibit relatively high wet anddry resilience. Dry crosslinked fibers are further characterized by lowfluid retention values (FRV).

Processes for producing aqueous solution crosslinked fibers aredisclosed, for example, in U.S. Pat. No. 3,241,553, F. H. Steiger,issued Mar. 22, 1966. Individualized, crosslinked fibers are produced bycrosslinking the fibers in an aqueous solution containing a crosslinkingagent and a catalyst. Fibers produced in this manner are hereinafterreferred to as "aqueous solution crosslinked" fibers. Due to theswelling effect of water on cellulosic fibers, aqueous solutioncrosslinked fibers are crosslinked while in an uncollapsed, swollenstate. Relative to dry crosslinked fibers, aqueous solution crosslinkedfibers as disclosed in U.S. Pat. No. 3,241,553 have greater flexibilityand less stiffness, and are characterized by higher fluid retentionvalue (FRV). Absorbent structures made from aqueous solution crosslinkedfibers exhibit lower wet and dry resilience than structures made fromdry crosslinked fibers.

In U.S. Pat. No, 4,035,147, Sangenis et al., issued Jul. 12, 1977, amethod is disclosed for producing individualized, crosslinked fibers bycontacting dehydrated, nonswollen fibers with crosslinking agent andcatalyst in a substantially nonaqueous solution which contains aninsufficient amount of water to cause the fibers to swell. Crosslinkingoccurs while the fibers are in this substantially nonaqueous solution.This type of process shall hereinafter be referred to as a nonaqueoussolution crosslinked process; and the fibers thereby produced shall bereferred to as nonaqueous solution crosslinked fibers. The nonaqueoussolution crosslinked fibers disclosed in U.S. Pat. No. 4,035,147 do notswell even upon extended contact with solutions known to those skilledin the art as swelling reagents. Like dry crosslinked fibers, they arehighly stiffened by crosslink bonds, and absorbent structures madetherefrom exhibit relatively high wet and dry resilience.

Crosslinked fibers as described above are believed to be useful forlower density absorbent product applications such as diapers and alsohigher density absorbent product applications such as catamenials.However, such fibers have not provided sufficient absorbency benefits,in view of their detriments and costs, over conventional fibers toresult in significant commercial success. Commercial appeal ofcrosslinked fibers has also suffered due to safety concerns. Thecrosslinking agents most widely referred to in the literature areformaldehyde and formaldehyde addition products known as N-methylolagents or N-methylolamides, which, unfortunately, cause irritation tohuman skin and have been associated with other human safety concerns.Removal of free formaldehyde to sufficiently low levels in thecrosslinked product such that irritation to skin and other human safetyconcerns are avoided has been hindered by both technical and economicbarriers.

As mentioned above, the use of formaldehyde and various formaldehydeaddition products to crosslink cellulosic fibers is known in the art.See, for example, U.S. Pat. No. 3,224,926, Bernardin, issued on Dec. 21,1965; U.S. Pat. No. 3,241,553, Steiger, issued on Mar. 22, 1966; U.S.Pat. No. 3,932,209, Chatterjee, issued on Jan. 13, 1976; U.S. Pat. No.4,035,147, Sangenis et al, issued on Jul. 12, 1977; and U.S. Pat. No.3,756,913, Wodka, issued on Sep. 4, 1973. Unfortunately, the irritatingeffect of formaldehyde vapor on the eyes and skin is a markeddisadvantage of such references. A need is evident for cellulosic fibercrosslinking agents that do not require formaldehyde or its unstablederivatives.

Other references disclose the use of dialdehyde crosslinking agents.See, for example, U.S. Pat. No. 4,689,118, Makoui et al, issued on Aug.25, 1987; and U.S. Pat. No. 4,822,453, Dean et al, issued on Apr. 18,1989. The Dean et al reference discloses absorbent structures containingindividualized, crosslinked fibers, wherein the crosslinking agent isselected from the group consisting of C₂ -C₈ dialdehydes, withglutaraldehyde being preferred. These references appear to overcome manyof the disadvantages associated with formaldehyde and/or formaldehydeaddition products. However, the cost associated with producing fiberscrosslinked with dialdehyde crosslinking agents such as glutaraldehydemay be too high to result in significant commercial success. Therefore,there is a need to find cellulosic fiber crosslinking agents which areboth safe for use on the human skin and also commercially feasible.

The use of polycarboxylic acids to impart wrinkle resistance to cottonfabrics is known in the art. See, for example, U.S. Pat. No. 3,526,048,Roland et al, issued Sep. 1, 1970; U.S. Pat. No. 2,971,815, Bullock etal, issued Feb. 14, 1961 and U.S. Pat. No. 4,820,307, Welch et al,issued Apr. 11, 1989. These references all pertain to treating cottontextile fabrics with polycarboxylic acids and specific curing catalyststo improve the wrinkle resistance and durability properties of thetreated fabrics.

It has now been discovered that ester crosslinks can be imparted ontoindividualized cellulosic fibers through the use of specificpolycarboxylic acid crosslinking agents. The ester crosslink bondsformed by the polycarboxylic acid crosslinking agents are different fromthe crosslink bonds that result from the mono- and di-aldehydecrosslinking agents, which form acetal crosslinked bonds. Applicantshave found that absorbent structures made from these individualized,ester-crosslinked fibers exhibit increased wet resilience and dryresilience and improved responsiveness to wetting relative to structurescontaining uncrosslinked fibers. Importantly, the polycarboxylic acidsdisclosed for use in the present invention, are nontoxic, unlikeformaldehyde and formaldehyde addition products commonly used in theart. Furthermore, the preferred polycarboxylic crosslinking agent i.e.,citric acid, is available in large quantities at relatively low pricesmaking it commercially competitive with the aldehyde crosslinkingagents, without any of the related human safety concerns.

It is an object of this invention to provide individualized fiberscrosslinked with a polycarboxylic acid crosslinking agent and absorbentstructures made from such fibers wherein the absorbent structures madefrom the crosslinked fibers have higher levels of absorbent capacityrelative to absorbent structures made from uncrosslinked fibers, andexhibit higher wet resilience and higher dry resilience than structuresmade from uncrosslinked fibers.

It is a further object of this invention to provide individualizedfibers crosslinked with a polycarboxylic crosslinking agent andabsorbent structures made from such fibers, as described above, whichhave a superior balance of absorbency properties relative to prior knowncrosslinked fibers.

It is additionally an object of this invention to provide commerciallyviable individualized, crosslinked fibers and absorbent structures madefrom such fibers, as described above, which can be safely utilized inthe vicinity of human skin.

It is another object of this invention to provide absorbent structureshaving improved absorbent capacity and wicking which, in actual use,provide high levels of wearer skin dryness.

SUMMARY OF THE INVENTION

It has been found that the objects identified above may be met byindividualized, crosslinked fibers and incorporation of these fibersinto absorbent structures, as disclosed herein. Preferably, theindividualized, crosslinked fibers having between about 0.5 mole % andabout 10.0 mole %, more preferably between about 1.5 mole % and about6.0 mole % crosslinking agent, calculated on a cellulose anhydroglucosemolar basis, reacted with the fibers in the form of intrafiber crosslinkbonds wherein the crosslinking agent is selected from the groupconsisting of C₂ -C₉ polycarboxylic acids. The crosslinking agent isreacted with the fibers in an intrafiber crosslinking bond form. Suchfibers, which are characterized by having water retention values (WRV's)of from about 25 to about 60, more preferably from about 28 to about 50,have been found to fulfill the identified objects relating toindividualized, crosslinked fibers and provide unexpectedly goodabsorbent performance in absorbent structure applications.

The individualized, crosslinked fibers are, without limiting the scopeof the invention, preferably formed into compressed absorbent structuresthat expand upon wetting.

The absorbent structures may additionally contain hydrogel-formingmaterial. Significantly improved skin dryness and absorbent capacity andskin dryness of the wearer may be obtained with the utilization ofhydrogel-forming material with individualized, crosslinked fibers.Significantly improved wicking and absorbent capacity are obtained byutilizing individualized, crosslinked fibers with hydrogel-formingmaterial relative to utilizing conventional, uncrosslinked cellulosefibers with hydrogel-forming material. Surprisingly, such improvedresults may be obtained pursuant to the utilization of lower levels ofhydrogel-forming material, calculated weight basis, for individualized,crosslinked fiber-containing pads compared to conventional cellulosicfiber pads.

DETAILED DESCRIPTION OF THE INVENTION

Cellulosic fibers of diverse natural origin are applicable to theinvention. Digested fibers from softwood, hardwood or cotton linters arepreferably utilized. Fibers from Esparto grass, bagasse, kemp, flax, andother lignaceous and cellulosic fiber sources may also be utilized asraw material in the invention. The fibers may be supplied in slurry,unsheeted or sheeted form. Fibers supplied as wet lap, dry lap or othersheeted form are preferably rendered into unsheeted form by mechanicallydisintegrating the sheet, preferably prior to contacting the fibers withthe crosslinking agent. Also, preferably the fibers are provided in awet or moistened condition. Most preferably, the fibers are never-driedfibers. In the case of dry lap, it is advantageous to moisten the fibersprior to mechanical disintegration in order to minimize damage to thefibers.

The optimum fiber source utilized in conjunction with this inventionwill depend upon the particular end use contemplated. Generally, pulpfibers made by chemical pulping processes are preferred. Completelybleached, partially bleached and unbleached fibers are applicable. Itmay frequently be desired to utilize bleached pulp for its superiorbrightness and consumer appeal. For products such as paper towels andabsorbent pads for diapers, sanitary napkins, catamenials, and othersimilar absorbent paper products, it is especially preferred to utilizefibers from southern softwood pulp due to their premium absorbencycharacteristics.

Crosslinking agents applicable to the present development includealiphatic and alicyclic C₂ -C₉ polycarboxylic acids. As used herein, theterm "C₂ -C₉ polycarboxylic acid" refers to an organic acid containingtwo or more carboxyl (COOH) groups and from 2 to 9 carbon atoms in thechain or ring to which the carboxyl groups are attached. The carboxylgroups are not included when determining the number of carbon atoms inthe chain or ring. For example, 1,2,3 propane tricarboxylic acid wouldbe considered to be a C₃ polycarboxylic acid containing three carboxylgroups. Similarly, 1,2,3,4 butane tetracarboxylic acid would beconsidered to be a C₄ polycarboxylic acid containing four carboxylgroups.

More specifically, the C₂ -C₉ polycarboxylic acids suitable for use ascellulose crosslinking agents in the present invention include aliphaticand alicyclic acids either olefinically saturated or unsaturated with atleast three and preferably more carboxyl groups per molecule or with twocarboxyl groups per molecule if a carbon-carbon double bond is presentalpha, beta to one or both carboxyl groups. An additional requirement isthat to be reactive in esterifying cellulose hydroxyl groups, a givencarboxyl group in an aliphatic or alicyclic polycarboxylic acid must beseparated from a second carboxyl group by no less than 2 carbon atomsand no more than three carbon atoms. Without being bound by theory, itappears from these requirements that for a carboxyl group to bereactive, it must be able to form a cyclic 5- or 6-membered anhydridering with a neighboring carboxyl group in the polycarboxylic acidmolecule. Where two carboxyl groups are separated by a carbon-carbondouble bond or are both connected to the same ring, the two carboxylgroups must be in the cis configuration relative to each other if theyare to interact in this manner.

In aliphatic polycarboxylic acids containing three or more carboxylgroups per molecule, a hydroxyl group attached to a carbon atom alpha toa carboxyl group does not interfere with the esterification andcrosslinking of the cellulosic fibers by the acid. Thus, polycarboxylicacids such as citric acid (also known as 2-hydroxy-1,2,3 propanetricarboxylic acid) and tartrate monosuccinic acids are suitable ascrosslinking agents in the present development.

The aliphatic or alicyclic C₂ -C₉ polycarboxylic acid crosslinkingagents may also contain an oxygen or sulfur atom(s) in the chain or ringto which the carboxyl groups are attached. Thus, polycarboxylic acidssuch as oxydisuccinic acid also known as 2,2'-oxybis(butanedioic acid),thiodisuccinic acid, and the like, are meant to be included within thescope of the invention. For purposes of the present invention,oxydisuccinic acid would be considered to be a C₄ polycarboxylic acidcontaining four carboxyl groups.

Examples of specific polycarboxylic acids which fall within the scope ofthis invention include the following: maleic acid, citraconic acid alsoknown as methylmaleic acid, citric acid, itaconic acid also known asmethylenesuccinic acid, tricarballylic acid also known as 1,2,3 propanetricarboxylic acid, transaconitic acid also known astrans-1-propene-1,2,3-tricarboxylic acid, 1,2,3,4-butanetetracarboxylicacid, all-cis-1,2,3,4-cyclopentanetetracarboxylic acid, mellitic acidalso known as benzenehexacarboxylic acid, and oxydisuccinic acid alsoknown as 2,2'-oxybis(butanedioic acid). The above list of specificpolycarboxylic acids is for exemplary purposes only, and is not intendedto be all inclusive. Importantly, the crosslinking agent must be capableof reacting with at least two hydroxyl groups on proximately locatedcellulose chains in a single cellulosic fiber.

Preferably, the C₂ -C₉ polycarboxylic acids used herein are aliphatic,saturated, and contain at least three carboxyl groups per molecule. Onegroup of preferred polycarboxylic acid crosslinking agents for use withthe present invention include citric acid also known as 2-hydroxy-1,2,3propane tricarboxylic acid, 1,2,3 propane tricarboxylic acid, and1,2,3,4 butane tetracarboxylic acid. Citric acid is especiallypreferred, since it has provided fibers with high levels of absorbencyand resiliency, is safe and non-irritating to human skin, an hasprovided stable, crosslink bonds. Furthermore, citric acid is availablein large quantities at relatively low prices, thereby making itcommercially feasible for use as a crosslinking agent.

Another group of preferred crosslinking agents for use in the presentinvention includes saturated C₂ -C₉ polycarboxylic acids containing atleast one oxygen atom in the chain to which the carboxyl groups areattached. Examples of such compounds include oxydisuccinic acid,tartrate monosuccinic acid having the structural formula: ##STR1## andtartrate disuccinic acid having the structural formula: ##STR2## A moredetailed description of tartrate monosuccinic acid, tartrate disuccinicacid, and salts thereof, can be found in U.S. Pat. No. 4,663,071, Bushet al., issued May 5, 1987, incorporated herein by reference.

Those knowledgeable in the area of polycarboxylic acids will recognizethat the aliphatic and alicyclic C₂ -C₉ polycarboxylic acid crosslinkingagents described above may be present in a variety of forms, such as thefree acid form, and salts thereof. Although the free acid form ispreferred, all such forms are meant to be included within the scope ofthe invention.

The individualized, crosslinked fibers used in the absorbent structuresof the present invention have an effective amount of the C₂ -C₉polycarboxylic acid crosslinking agent reacted with the fibers in theform of intrafiber crosslink bonds. As used herein, "effective amount ofcrosslinking agent" refers to an amount of crosslinking agent sufficientto provide an improvement in at least one significant absorbencyproperty of the fibers themselves and/or absorbent structures containingthe individualized, crosslinked fibers, relative to conventional,uncrosslinked fibers. One example of a significant absorbency propertyis drip capacity, which is a combined measurement of an absorbentstructure's fluid absorbent capacity and fluid absorbency rate. Adetailed description of the procedure for determining drip capacity isprovided hereinafter.

In particular, unexpectedly good results are obtained for absorbent padsmade from individualized, crosslinked fibers having between about 0.5mole % and about 10.0 mole %, more preferably between about 1.5 mole %and about 6.0 mole % crosslinking agent, calculated on a celluloseanhydroglucose molar basis, reacted with the fibers.

Preferably, the crosslinking agent is contacted with the fibers in aliquid medium, under such conditions that the crosslinking agentpenetrates into the interior of the individual fiber structures.However, other methods of crosslinking agent treatment, includingspraying of the fibers while in individualized, fluffed form, are alsowithin the scope of the invention.

Applicants have discovered that the crosslinking reaction can beaccomplished at practical rates without a catalyst, provided the pH iskept within a particular range (to be discussed in more detail below).This is contrary to the prior art which teaches that specific catalystsare needed to provide sufficiently rapid esterification and crosslinkingof fibrous cellulose by polycarboxylic acid crosslinking agents to becommercially feasible. See, for example, U.S. Pat. No. 4,820,307, Welchet al., issued Apr. 11, 1989.

However, if desired, the fibers can also be contacted with anappropriate catalyst prior to crosslinking. Applicants have found thatthe type, amount, and method of contact of catalyst to the fibers willbe dependent upon the particular crosslinking process practiced. Thesevariables will be discussed in more detail below.

Once the fibers are treated with crosslinking agent (and catalyst if oneis used), the crosslinking agent is caused to react with the fibers inthe substantial absence of interfiber bonds, i.e., while interfibercontact is maintained at a low degree of occurrence relative tounfluffed pulp fibers, or the fibers are submerged in a solution thatdoes not facilitate the formation of interfiber bonding, especiallyhydrogen bonding. This results in the formation of crosslink bonds whichare intrafiber in nature. Under these conditions, the crosslinking agentreacts to form crosslink bonds between hydroxyl groups of a singlecellulose chain or between hydroxyl groups of proximately locatedcellulose chains of a single cellulosic fiber.

Although not presented or intended to limit the scope of the invention,it is believed that the carboxyl groups on the polycarboxylic acidcrosslinking agent react with the hydroxyl groups of the cellulose toform ester bonds. The formation of ester bonds, believed to be thedesirable bond type providing stable crosslink bonds, is favored underacidic reaction conditions. Therefore, acidic crosslinking conditions,i.e. pH ranges of from about 1.5 to about 5, are highly preferred forthe purposes of this invention.

The fibers are preferably mechanically defibrated into a low density,individualized, fibrous form known as "fluff" prior to reaction of thecrosslinking agent with the fibers. Mechanical defibration may beperformed by a variety of methods which are presently known in the artor which may hereafter become known. Mechanical defibration ispreferably performed by a method wherein knot formation and fiber damageare minimized. One type of device which has been found to beparticularly useful for defibrating the cellulosic fibers is the threestage fluffing device described in U.S. Pat. No. 3,987,968, issued to D.R. Moore and O. A. Shields on Oct. 26, 1976, said patent being herebyexpressly incorporated by reference into this disclosure. The fluffingdevice described in U.S. Pat. No. 3,987,968 subjects moist cellulosicpulp fibers to a combination of mechanical impact, mechanical agitation,air agitation and a limited amount of air drying to create asubstantially knot-free fluff. The individualized fibers have impartedthereto an enhanced degree of curl and twist relative to the amount ofcurl and twist naturally present in such fibers. It is believed thatthis additional curl and twist enhances the resilient character ofabsorbent structures made from the finished, crosslinked fibers.

Other applicable methods for defibrating the cellulosic fibers include,but are not limited to, treatment with a Waring blender and tangentiallycontacting the fibers with a rotating disk refiner or wire brush.Preferably, an air stream is directed toward the fibers during suchdefibration to aid in separating the fibers into substantiallyindividual form.

Regardless of the particular mechanical device used to form the fluff,the fibers are preferably mechanically treated while initiallycontaining at least about 20% moisture, and preferably containingbetween about 40% and about 65% moisture.

Mechanical refining of fibers at high consistency or of partially driedfibers may also be utilized to provide curl or twist to the fibers inaddition to curl or twist imparted as a result of mechanicaldefibration.

The fibers made according to the present invention have uniquecombinations of stiffness and resiliency, which allow absorbentstructures made from the fibers to maintain high levels of absorptivity,and exhibit high levels of resiliency and an expansionary responsivenessto wetting of a dry, compressed absorbent structure. In addition tohaving the levels of crosslinking within the stated ranges, thecrosslinked fibers are characterized by having water retention values(WRV's) of less than about 60, preferably from about 28 to about 50, andmore preferably between about 30 and about 45, for conventional,chemically pulped, papermaking fibers. The WRV of a particular fiber isindicative of the level .of crosslinking. Very highly crosslinkedfibers, such as those produced by many of the prior art knowncrosslinking processes previously discussed, have been found to haveWRV's of less than about 25, and generally less than about 20. Theparticular crosslinking process utilized will, of course, affect the WRVof the crosslinked fiber. However, any process which will result incrosslinking levels and WRV's within the stated limits is believed tobe, and is intended to be, within the scope of this invention.Applicable methods of crosslinking include dry crosslinking processesand nonaqueous solution crosslinking processes as generally discussed inthe Background Of The Invention. Certain preferred dry crosslinking andnonaqueous solution crosslinking processes for preparing theindividualized, crosslinked fibers of the present invention, will bediscussed in more detail below. Aqueous solution crosslinking processeswherein the solution causes the fibers to become highly swollen willresult in fibers having WRV's which are in excess of about 60. Thesefibers will provide insufficient stiffness and resiliency for thepurposes of the present invention.

Specifically referring to dry crosslinking processes, individualized,crosslinked fibers may be produced from such a process by providing aquantity of cellulosic fibers, contacting a slurry of the fibers with atype and amount of crosslinking agent as described above, mechanicallyseparating, e.g., defibrating, the fibers into substantially individualform, and drying the fibers and causing the crosslinking agent to reactwith the fibers in the presence of a catalyst to form crosslink bondswhile the fibers are maintained in substantially individual form. Thedefibration step, apart from the drying step, is believed to impartadditional curl. Subsequent drying is accompanied by twisting of thefibers, with the degree of twist being enhanced by the curled geometryof the fiber. As used herein, fiber "curl" refers to a geometriccurvature of the fiber about the longitudinal axis of the fiber. "Twist"refers to a rotation of the fiber about the perpendicular cross-sectionof the longitudinal axis of the fiber. The fibers of the preferredembodiment of the present invention are individualized, crosslinked inintrafiber bond form, and are highly twisted and curled.

As used herein, the term "twist count" refers to the number of twistnodes present in a certain length of fiber. Twist count is utilized as ameans of measuring the degree to which a fiber is rotated about itslongitudinal axis. The term "twist node" refers to a substantially axialrotation of 180° about the longitudinal axis of the fiber, wherein aportion of the fiber (i.e., the "node") appears dark relative to therest of the fiber when viewed under a microscope with transmitted light.The distance between nodes corresponds to an axial rotation of 180°.Those skilled in the art will recognize that the occurrence of a twistnode as described above, is primarily a visual rather than a physicalphenomena. However, the number of twist nodes in a certain length offibers (i.e., the twist count) is directly indicative of the degree offiber twist, which is a physical parameter of the fiber. The appearanceand quantity of twist nodes will vary depending upon whether the fiberis a summerwood fiber or a springwood fiber. The twist nodes and totaltwist count are determined by a Twist Count Image Analysis Method whichis described in the Experimental Method section of the disclosure. Theaverage twist count referred to in describing the fibers of the presentinvention is properly determined by the aforementioned twist countmethod. When counting twist nodes, portions of fiber darkened due tofiber damage or fiber compression should be distinguished from portionsof fiber appearing darkened due to fiber twisting.

The actual twist count of any given sample of fibers will vary dependingupon the ratio of springwood fibers to summerwood fibers. The twistcount of any particular springwood or summerwood fibers will also varyfrom fiber to fiber. Notwithstanding the above, the average twist countlimitations are useful in defining the invention, and these limitationsapply regardless of the particular combination of springwood fibers andsummerwood fibers. That is, any mass of fibers having twist countencompassed by the stated twist count limitations are meant to beencompassed within the scope of the present invention, so long as theother claimed limitations are met.

In the measurement of twist count for a sample of fibers, it isimportant that a sufficient amount of fibers be examined in order toaccurately represent the average level of twist of the variableindividual fiber twist levels. It is suggested that at least five (5)inches of cumulative fiber length of a representative sample of a massof fibers be tested in order to provide a representative fiber twistcount.

The wet fiber twist count is described and measured analogously to thedry fiber twist count, said method varying only in that the fiber iswetted with water prior to being treated and the twist nodes are thencounted while wet in accordance with the Twist Count Image AnalysisMethod.

Preferably, the average dry fiber twist count is at least about 2.5twist nodes per millimeter, and the average wet fiber twist count is atleast about 1.5 twist nodes per millimeter and is at least 1.0 twistnodes per millimeter less than its dry fiber twist count. Mostpreferably, the average dry fiber twist count is at least about 3.0twist nodes per millimeter, and the average wet fiber twist count is atleast about 2.0 twist nodes per millimeter and is at least 1.0 twistnodes per millimeter less than the dry fiber twist count.

In addition to being twisted, the fibers of the present invention arecurled. Fiber curl may be described as a fractional shortening of thefiber due to kinks, twists, and/or bends in the fiber. For the purposesof this disclosure, fiber curl shall be measured in terms of a twodimensional field. The level of fiber curl shall be referred to in termsof a fiber curl index. The fiber curl factor, a two dimensionalmeasurement of curl, is determined by viewing the fiber in a twodimensional plane, measuring the projected length of the fiber as thelongest dimension of a rectangle encompassing the fiber, L_(R), and theactual length of the fiber L_(A), and then calculating the fiber curlfactor from the following equation:

    Curl Factor=(L.sub.A /L.sub.R)-1                           (1)

A Fiber Curl Index Image Analysis Method is utilized to measure L_(R)and L_(A). This method is described in the Experimental Methods sectionof this disclosure. The background information for this method isdescribed in the 1979 International Paper Physics Conference Symposium,The Harrison Hotel, Harrison Hot Springs, British Columbia, Sep. 17-19,1979 in a paper titled "Application Of Image Analysis To Pulp FibreCharacterization: Part 1," by B. D. Jordan and D. H. Page, pp. 104-114,Canadian Pulp and Paper Association (Montreal, Quebec, Canada), saidreference being incorporated by reference into this disclosure.

Preferably, the fibers have a curl factor of at least about 0.30, andmore preferably of at least about 0.50.

Maintaining the fibers in substantially individual form during dryingand crosslinking allows the fibers to twist during drying and thereby becrosslinked in such twisted, curled state. Drying fibers under suchconditions that the fibers may twist and curl is referred to as dryingthe fibers under substantially unrestrained conditions. On the otherhand, drying fibers in sheeted form results in dried fibers which arenot as highly twisted and curled as fibers dried in substantiallyindividualized form. It is believed that interfiber hydrogen bonding"restrains" the relative occurrence of twisting and curling of thefiber.

There are various methods by which the fibers may be contacted with thecrosslinking agent and catalyst (if a catalyst is used). In oneembodiment, the fibers are contacted with a solution which initiallycontains both the crosslinking agent and the catalyst. In anotherembodiment, the fibers are contacted with an aqueous solution ofcrosslinking agent and allowed to soak prior to addition of thecatalyst. The catalyst is subsequently added. In a third embodiment, thecrosslinking agent and catalyst are added to an aqueous slurry of thecellulosic fibers. Other methods in addition to those described hereinwill be apparent to those skilled in the art, and are intended to beincluded within the scope of this invention. Regardless of theparticular method by which the fibers are contacted with crosslinkingagent and catalyst (if a catalyst is used), the cellulosic fibers,crosslinking agent and catalyst are preferably mixed and/or allowed tosoak sufficiently with the fibers to assure thorough contact with andimpregnation of the individual fibers.

Applicants have discovered that the crosslinking reaction can beaccomplished without the use of a catalyst if the pH of the solutioncontaining the crosslinking agent is kept within the ranges specifiedhereinafter. In particular, the aqueous portion of the cellulosic fiberslurry or crosslinking agent solution should be adjusted to a target pHof between about pH 1.5 and about pH 5, more preferably between about pH2.0 and about pH 3.5, during the period of contact between thecrosslinking agent and the fibers. Preferably, the pH is adjusted by theaddition of a base, such as sodium hydroxide, to the crosslinking agentsolution.

Notwithstanding the above, in general, any substance which can catalyzethe crosslinking mechanism may be utilized. Applicable catalysts includealkali metal hypophosphites, alkali metal phosphites, alkali metalpolyphosphates, alkali metal phosphates, and alkali metal sulfates.Especially preferred catalysts are the alkali metal hypophosphites,alkali metal phosphates, and alkali metal sulfates. The mechanism of thecatalysis is unknown, although applicants believe that the catalysts maysimply be functioning as buffering agents, keeping the pH levels withinthe desired ranges. A more complete list of catalysts useful herein canbe found in U.S. Pat. No. 4,820,307, Welch et al, issued April 1989,incorporated herein by reference. The selected catalyst may be utilizedas the sole catalyzing agent, or in combination with one or more othercatalysts.

The amount of catalyst preferably utilized is, of course, dependent uponthe particular type and amount of crosslinking agent and the reactionconditions, especially temperature and pH. In general, based upontechnical and economic considerations, catalyst levels of between about5 wt. % and about 80 wt. %, based on the weight of crosslinking agentadded to the cellulosic fibers, are preferred. For exemplary purposes,in the case wherein the catalyst utilized is sodium hypophosphite andthe crosslinking agent is citric acid, a catalyst level of about 50 wt.%, based upon the amount of citric acid added, is preferred. It isadditionally desirable to adjust the aqueous portion of the cellulosicfiber slurry or crosslinking agent solution to a target pH of betweenabout pH 1.5 and about pH 5, more preferably between about pH 2.0 andabout pH 3.5, during the period of contact between the crosslinkingagent and the fibers.

The cellulosic fibers should generally be dewatered and optionallydried. The workable and optimal consistencies will vary depending uponthe type of fluffing equipment utilized. In the preferred embodiments,the cellulosic fibers are dewatered and optimally dried to a consistencyof between about 20% and about 80%. More preferably, the fibers aredewatered and dried to a consistency level of between about 35% andabout 60%. Drying the fibers to within these preferred ranges generallywill facilitate defibration of the fibers into individualized formwithout excessive formation of knots associated with higher moisturelevels and without high levels of fiber damage associated with lowermoisture levels.

For exemplary purposes, dewatering may be accomplished by such methodsas mechanically pressing, centrifuging, or air drying the pulp.Additional drying of the fibers within the 35-60% consistency rangepreviously described is optional but is preferably performed by amethod, known in the art as air drying, under conditions such that theutilization of high temperature for an extended period of time is notrequired. Excessively high temperature and time in this stage may resultin drying the fibers beyond 60% consistency, thereby possibly producingexcessive fiber damage during the ensuing defibration stage. Afterdewatering, the fibers are then mechanically defibrated as previouslydescribed.

The defibrated fibers are then dried to between 60% and 100% consistencyby a method known in the art as flash drying. This stage impartsadditional twist and curl to the fibers as water is removed from them.While the amount of water removed by this additional drying step may bevaried, it is believed that flash drying to higher consistency providesa greater level of fiber twist and curl than does flash drying to aconsistency in the lower part of the 60%-100% range. In the preferredembodiments, the fibers are dried to about 90%-95% consistency. It isbelieved that this level of flash drying provides the desired level offiber twist and curl without requiring the higher flash dryingtemperatures and retention times required to reach 100% consistency.Flash drying the fibers to a consistency, such as 90%-95%, in the higherportion of the 60%-100% range also reduces the amount of drying whichmust be accomplished in the curing stage following flash drying.

The flash dried fibers are then heated to a suitable temperature for aneffective period of time to cause the crosslinking agent to cure, i.e.,to react with the cellulosic fibers. The rate and degree of crosslinkingdepends upon dryness of the fiber, temperature, pH, amount and type ofcatalyst and crosslinking agent and the method utilized for heatingand/or drying the fibers while crosslinking is performed. Crosslinkingat a particular temperature will occur at a higher rate for fibers of acertain initial moisture content when accompanied by a continuous,air-through drying than when subjected to drying/heating in a staticoven. Those skilled in the art will recognize that a number oftemperature-time relationships exist for the curing of the crosslinkingagent. Drying temperatures from about 145° C. to about 165° C. forperiods of between about 30 minutes and 60 minutes, under static,atmospheric conditions will generally provide acceptable curingefficiencies for fibers having moisture contents less than about 10%.Those skilled in the art will also appreciate that higher temperaturesand forced air convection decrease the time required for curing. Thus,drying temperatures from about 170° C. to about 190° C. for periods ofbetween about 2 minutes and 20 minutes, in an air-through oven will alsogenerally provide acceptable curing efficiencies for fibers havingmoisture contents less than about 10%. Curing temperatures should bemaintained at less than about 225° C., preferably less than about 200°C., since exposure of the fibers to such high temperatures may lead todarkening or other damaging of the fibers.

Without being bound by theory, it is believed that the chemical reactionof the cellulosic fibers with the C₂ -C₉ polycarboxylic acidcrosslinking agent does not begin until the mixture of these materialsis heated in the curing oven. During the cure stage, ester crosslinkbonds are formed between the C₂ -C₉ polycarboxylic acid crosslinkingagent and the cellulose molecules. These ester crosslinkages are mobileunder the influence of heat, due to a transesterification reaction whichtakes place between ester groups and adjacent unesterified hydroxylgroups on the cellulosic fibers. It is further believed that the processof transesterification, which occurs after the initial ester bonds areformed, results in fibers which have improved absorbency propertiescompared to fibers that are not cured sufficiently to allowtransesterification to occur.

Following the crosslinking step, the fibers are washed, if desired.After washing, the fibers are defluidized and dried. The fibers whilestill in a moist condition may be subjected to a second mechanicaldefibration step which causes the crosslinked fibers to twist and curlbetween the defluidizing and drying steps. The same apparatuses andmethods previously described for defibrating the fibers are applicableto this second mechanical defibration step. As used in this paragraph,the term "defibration" refers to any of the procedures which may be usedto mechanically separate the fibers into substantially individual form,even though the fibers may already be provided in such form."Defibration" therefore refers to the step of mechanically treating thefibers, in either individual form or in a more compacted form, whereinsuch mechanical treatment step a) separates the fibers intosubstantially individual form if they were not already in such form, andb) imparts curl and twist to the fibers upon drying.

This second defibration treatment, after the fibers have beencrosslinked, is believed to increase the twisted, curled character ofthe pulp. This increase in the twisted, curled configuration of thefibers leads to enhanced absorbent structure resiliency andresponsiveness to wetting.

The maximum level of crosslinking will be achieved when the fibers areessentially dry (having less than about 5% moisture). Due to thisabsence of water, the fibers are crosslinked while in a substantiallyunswollen, collapsed state. Consequently, they characteristically havelow fluid retention values (FRV) relative to the range applicable tothis invention. The FRV refers to the amount of fluid calculated on adry fiber basis, that remains absorbed by a sample of fibers that havebeen soaked and then centrifuged to remove interfiber fluid. (The FRV isfurther defined and the Procedure For Determining FRV, is describedbelow.) The amount of fluid that the crosslinked fibers can absorb isdependent upon their ability to swell upon saturation or, in otherwords, upon their interior diameter or volume upon swelling to a maximumlevel. This, in turn, is dependent upon the level of crosslinking. Asthe level of intrafiber crosslinking increases for a given fiber andprocess, the FRV of the fiber will decrease. Thus, the FRV value of afiber is structurally descriptive of the physical condition of the fiberat saturation. Unless otherwise expressly indicated, FRV data describedherein shall be reported in terms of the water retention value (WRV) ofthe fibers. Other fluids, such as salt water and synthetic urine, mayalso be advantageously utilized as a fluid medium for analysis.Generally, the FRV of a particular fiber crosslinked by procedureswherein curing is largely dependent upon drying, such as the presentprocess, will be primarily dependent upon the crosslinking agent and thelevel of crosslinking. The WRV's of fibers crosslinked by this drycrosslinking process at crosslinking agent levels applicable to thisinvention are generally less than about 60, greater than about 28,preferably less than about 50, and more preferably between about 30 andabout 45. Bleached SSK fibers having between about 1.5 mole % and about6.0 mole % citric acid reacted thereon, calculated on a celluloseanhydroglucose molar basis, have been observed to have WRV'srespectively ranging from about 28 to about 40. The degree of bleachingand the practice of post-crosslinking bleaching steps have been found toaffect WRV. Southern softwood Kraft (SSK) fibers prepared by many of theprior art known crosslinking processes have levels of crosslinkinghigher than described herein, and have WRV's less than about 25. Suchfibers, as previously discussed, have been observed to be exceedinglystiff and to exhibit lower absorbent capabilities than the fibers of thepresent invention.

In another process for making individualized, crosslinked fibers by adry crosslinking process, cellulosic fibers are contacted with asolution containing a crosslinking agent as described above. Eitherbefore or after being contacted with the crosslinking agent, the fibersare provided in a sheet form. The fibers, while in sheeted form, aredried and caused to crosslink preferably by heating the fibers to atemperature of between about 120° C. and about 160° C. Subsequent tocrosslinking, the fibers are mechanically separated into substantiallyindividual form. This is preferably performed by treatment with a fiberfluffing apparatus such as the one described in U.S. Pat. No. 3,987,968or may be performed with other methods for defibrating fibers as may beknown in the art. The individualized, crosslinked fibers made accordingto this sheet crosslinking process are treated with a sufficient amountof crosslinking agent such that an effective amount of crosslinkingagent, preferably between about 0.5 mole % and about 10.0 mole %crosslinking agent, calculated on a cellulose anhydroglucose molar basisand measured subsequent to defibration, are reacted with the fibers inthe form of intrafiber crosslink bonds. Another effect of drying andcrosslinking the fibers while in sheet form is that fiber to fiberbonding restrains the fibers from twisting and curling with increaseddrying. Compared to individualized, crosslinked fibers made according toa process wherein the fibers are dried under substantially unrestrainedconditions and subsequently crosslinked in a twisted, curledconfiguration, absorbent structures containing the relatively untwistedfibers made by the sheet curing process described above would beexpected to exhibit lower wet resiliency and lower responsiveness towetting.

It is also contemplated to mechanically separate the fibers intosubstantially individual form between the drying and the crosslinkingstep. That is, the fibers are contacted with the crosslinking agent andsubsequently dried while in sheet form. Prior to crosslinking, thefibers are individualized to facilitate intrafiber crosslinking. Thisalternative crosslinking method, as well as other variations which willbe apparent to those skilled in the art, are intended to be within thescope of this invention.

Another category of crosslinking processes applicable to the presentinvention is nonaqueous solution cure crosslinking processes. The sametypes of fibers applicable to dry crosslinking processes may be used inthe production of nonaqueous solution crosslinked fibers. The fibers aretreated with a sufficient amount of crosslinking agent such that aneffective amount of crosslinking agent subsequently reacts with thefibers, and with an appropriate catalyst, if desired. The amounts ofcrosslinking agent and catalyst (if one is used) utilized will dependupon such reaction conditions as consistency, temperature, water contentin the crosslinking solution and fibers, type of crosslinking agent anddiluent in the crosslinking solution, and the amount of crosslinkingdesired. The crosslinking agent is caused to react while the fibers aresubmerged in a substantially nonaqueous solution. The nonaqueouscrosslinking solution contains a nonaqueous, water-miscible, polardiluent such as, but not limited to acetic acid, propanoic acid, oracetone. The crosslinking solution may also contain a limited amount ofwater or other fiber welling liquid, however, the amount of water ispreferably insufficient to induce any substantial levels of fiberswelling. Crosslinking solution systems applicable for use as acrosslinking medium include those disclosed in U.S. Pat. No. 4,035,147,issued to S. Sangenis, G. Guiroy, and J. Quere, on Jul. 12, 1977, whichis hereby incorporated by reference into this disclosure.

The crosslinked fibers used in the absorbent structures of the presentinvention are preferably prepared by the dry crosslinking processdiscussed above. The crosslinked fibers may be utilized directly in themanufacture of air laid absorbent cores. Additionally, due to theirstiffened and resilient character, the crosslinked fibers may be wetlaid into an uncompacted, low density sheet which, when subsequentlydried, is directly useful without further mechanical processing as anabsorbent core. The crosslinked fibers may also be wet laid as compactedpulp sheets for sale or transport to distant locations.

Relative to pulp sheets made from conventional, uncrosslinked cellulosicfibers, the pulp sheets made from the crosslinked fibers of the presentinvention are more difficult to compress to conventional pulp sheetdensities. Therefore, it may be desirable to combine crosslinked fiberswith uncrosslinked fibers, such as those conventionally used in themanufacture of absorbent cores. Pulp sheets containing stiffened,crosslinked fibers preferably contain between about 5% and about 90%uncrosslinked, cellulosic fibers, based upon the total dry weight of thesheet, mixed with the individualized, crosslinked fibers. It isespecially preferred to include between about 5% and about 30% of highlyrefined, uncrosslinked cellulosic fibers, based upon the total dryweight of the sheet. Such highly refined fibers are refined or beaten toa freeness level less than about 300 ml CSF, and preferably less than100 ml CSF. The uncrosslinked fibers are preferably mixed with anaqueous slurry of the individualized, crosslinked fibers. This mixturemay then be formed into a densified pulp sheet for subsequentdefibration and formation into absorbent pads. The incorporation of theuncrosslinked fibers eases compression of the pulp sheet into adensified form, while imparting a surprisingly small loss in absorbencyto the subsequently formed absorbent pads. The uncrosslinked fibersadditionally increase the tensile strength of the pulp sheet and toabsorbent pads made either from the pulp sheet or directly from themixture of crosslinked and uncrosslinked fibers. Regardless of whetherthe blend of crosslinked and uncrosslinked fibers are first made into apulp sheet and then formed into an absorbent pad or formed directly intoan absorbent pad, the absorbent pad may be air-laid or wet-laid.

Sheets or webs made from the individualized, crosslinked fibers, or frommixtures also containing uncrosslinked fibers, will preferably havebasis weights of less than about 800 g/m² and densities of less thanabout 0.60 g/cm³. Although it is not intended to limit the scope of theinvention, wet-laid sheets having basis weights between 300 g/m² andabout about 600 g/m² and densities between 0.07 g/cm³ and about 0.30g/cm³ are especially contemplated for direct application as absorbentcores in disposable articles such as diapers, tampons, and othercatamenial products. Structures having basis weights and densitieshigher than these levels are believed to be most useful for subsequentcomminution and air-laying or wet-laying to form a lower density andbasis weight structure which is more useful for absorbent applications.Although, such higher basis weight and density structures also exhibitsurprisingly high absorptivity and responsiveness to wetting. Otherapplications contemplated for the fibers of the present inventioninclude low density tissue sheets having densities which may be lessthan about 0.03 g/cc.

If desired, the crosslinked fibers can be further processed to removeexcess, unreacted crosslinking agent. One series of treatments found tosuccessfully remove excess crosslinking agent comprise, in sequence,washing the crosslinked fibers, allowing the fibers to soak in anaqueous solution for an appreciable time, screening the fibers,dewatering the fibers, e.g., by centrifuging, to a consistency ofbetween about 40% and about 80%, mechanically defibrating the dewateredfibers as previously described and air drying the fibers. A sufficientamount of an acidic substance may be added to the wash solution, ifnecessary, to keep the wash solution at a pH of less than about 7.Without being bound by theory, it is believed that the ester crosslinksare not stable under alkaline conditions and that keeping the washtreatment pH in the acidic range inhibits reversion of the estercrosslinks which have formed. Acidity may be introduced by mineral acidssuch as sulfuric acid, or alternatively in the form of acidic bleachchemicals such as chlorine dioxide and sodium hydrosulfite (which mayalso be added to brighten the crosslinked fibers). This process has beenfound to reduce residual free crosslinking agent content to betweenabout 0.01% and about 0.15%.

The crosslinked fibers herein described are useful for a variety ofabsorbent articles including, but not limited to, tissue sheets,disposable diapers, catamenials, sanitary napkins, tampons, and bandageswherein each of said articles has an absorbent structure containing theindividualized, crosslinked fibers described herein. For example, adisposable diaper or similar article having a liquid permeable topsheet,a liquid impermeable backsheet connected to the topsheet, and anabsorbent structure containing individualized, crosslinked fibers isparticularly contemplated. Such articles are described generally in U.S.Pat. No. 3,860,003, issued to Kenneth B. Buell on Jan. 14, 1975, herebyincorporated by reference into this disclosure.

Conventionally, absorbent cores for diapers and catamenials are madefrom unstiffened, uncrosslinked cellulosic fibers, wherein the absorbentcores have dry densities of about 0.06 g/cc and about 0.12 g/cc. Uponwetting, the absorbent core normally displays a reduction in volume.

It has been found that the crosslinked fibers of the present inventioncan be used to make absorbent cores having substantially higher fluidabsorbing properties including, but not limited to, absorbent capacityand wicking rate relative to equivalent density absorbent cores madefrom conventional, uncrosslinked fibers or prior known crosslinkedfibers. Furthermore, these improved absorbency results may be obtainedin conjunction with increased levels of wet resiliency. For absorbentcores having densities of between about 0.05 g/cc and about 0.15 g/ccwhich maintain substantially constant volume upon wetting, it isespecially preferred to utilize crosslinked fibers having crosslinkinglevels of between about 5.0 mole % and about 10.0 mole % crosslinkingagent, based upon a dry cellulose anhydroglucose molar basis. Absorbentcores made from such fibers have a desirable combination of structuralintegrity, i.e., resistance to compression, and wet resilience. The termwet resilience, in the present context, refers to the ability of amoistened pad to spring back towards its original shape and volume uponexposure to and release from compressional forces. Compared to coresmade from untreated fibers, and prior known crosslinked fibers, theabsorbent cores made from the fibers of the present invention willregain a substantially higher proportion of their original volumes uponrelease of wet compressional forces.

In another preferred embodiment, the individualized, crosslinked fibersare formed into either an air laid or wet laid (and subsequently dried)absorbent core which is compressed to a dry density less than theequilibrium wet density of the pad. The equilibrium wet density is thedensity of the pad, calculated on a dry fiber basis when the pad isfully saturated with fluid. When fibers are formed into an absorbentcore having a dry density less than the equilibrium wet density, uponwetting to saturation, the core will collapse to the equilibrium wetdensity. Alternatively, when fibers are formed into an absorbent corehaving a dry density greater than the equilibrium wet density, uponwetting to saturation, the core will expand to the equilibrium wetdensity. Pads made from the fibers of the present invention haveequilibrium wet densities which are substantially lower than pads madefrom conventional fluffed fibers. The fibers of the present inventioncan be compressed to a density higher than the equilibrium wet density,to form a thin pad which, upon wetting, will expand, thereby increasingabsorbent capacity, to a degree significantly greater than obtained foruncrosslinked fibers.

In another preferred embodiment, high absorbency properties, wetresilience, and responsiveness to wetting may be obtained forcrosslinking levels of between about 1.5 mole % and about 6.0 mole %,calculated on a dry cellulose molar basis. Preferably, such fibers areformed into absorbent cores having dry densities greater than theirequilibrium wet densities. Preferably, the absorbent cores arecompressed to densities of between about 0.12 g/cc and about 0.60 g/cc,wherein the corresponding equilibrium wet density is less than thedensity of the dry compressed pad. Also, preferably the absorbent coresare compressed to a density of between about 0.12 g/cc and about 0.40g/cc, wherein the corresponding equilibrium wet densities are betweenabout 0.08 g/cc and about 0.12 g/cc, and are less than the densities ofthe dry, compressed cores. It should be recognized, however, thatabsorbent structures within the higher density range can be made fromcrosslinked fibers having higher crosslinking levels, as can lowerdensity absorbent structures be made from crosslinked fibers havinglower levels of crosslinking. Improved performance relative to priorknown individualized, crosslinked fibers is obtained for all suchstructures.

While the foregoing discussion involves preferred embodiments for highand low density absorbent structures, it should be recognized that avariety of combinations of absorbent structure densities andcrosslinking agent levels between the ranges disclosed herein willprovide superior absorbency characteristics and absorbent structureintegrity relative to conventional cellulosic fibers and prior knowncrosslinked fibers. Such embodiments are meant to be included within thescope of this invention.

Absorbent structures made from individualized, crosslinked fibers mayadditionally contain discrete particles of substantiallywater-insoluble, hydrogel-forming material. Hydrogel-forming materialsare chemical compounds capable of absorbing fluids and retaining themunder moderate pressures.

Suitable hydrogel-forming materials can be inorganic materials such assilica gels or organic compounds such as crosslinked polymers. It shouldbe understood that crosslinking, when referred to in connection withhydrogel-forming materials, assumes a broader meaning than contemplatedin connection with the reaction of crosslinking agents with cellulosicfibers to form individualized, crosslinked fibers. Crosslinkedhydrogel-forming polymers may be crosslinked by covalent, ionic, Van derWaals, or hydrogen bonding. Examples of hydrogel-forming materialsinclude polyacrylamides, polyvinyl alcohol, ethylene maleic anhydridecopolymers, polyvinyl ethers, hydroxypropyl cellulose, carboxymethylcellulose, polyvinyl morpholinone, polymers and copolymers of vinylsulfonic acid, polyacrylates, polyacrylamides, polyvinyl pyridine andthe like. Other suitable hydrogel-forming materials are those disclosedin Assarsson et al., U.S. Pat. No. 3,901,236, issued Aug. 26, 1975, thedisclosure of which is incorporated herein by reference. Particularlypreferred hydrogel-forming polymers for use in the absorbent core arehydrolyzed acrylonitrile grafted starch, acrylic acid grafted starch,polyacrylates, and isobutylene maleic anhydride copolymers, or mixturesthereof. Examples of hydrogel-forming materials which may be used areAqualic L-73, a partially neutralized polyacrylic acid made by NipponShokubai Co., Japan, and Sanwet IM 1000, a partially neutralized acrylicacid grafted starch made by Sanyo Co., Ltd., Japan. Hydrogel formingmaterials having relatively high gel strengths, as described in U.S.Pat. No. 4,654,039, issued Mar. 31, 1987, hereby incorporated herein byreference, are preferred for utilization with individualized,crosslinked fibers.

Process for preparing hydrogel-forming materials are disclosed in Masudaet al., U.S. Pat. No. 4,076,663, issued Feb. 28, 1978; in Tsubakimoto etal., U.S. Pat. No. 4,286,082, issued Aug. 25, 1981; and further in U.S.Pat. Nos. 3,734,876, 3,661,815, 3,670,731, 3,664,343, 3,783,871, andBelgian Patent 785,850, the disclosures of which are all incorporatedherein by reference.

The hydrogel-forming material may be distributed throughout an absorbentstructure containing individualized, crosslinked fibers, or be limitedto distribution throughout a particular layer or section of theabsorbent structure. In another embodiment, the hydrogel-formingmaterial is adhered or laminated onto a sheet or film which isjuxtaposed against a fibrous, absorbent structure, which may includeindividualized, crosslinked fibers. Such sheet or film may bemultilayered such that the hydrogel-forming material is containedbetween the layers. In another embodiment, the hydrogel-forming materialmay be adhered directly onto the surface fibers of the absorbentstructure.

Surprisingly large increases in skin dryness have been observed forabsorbent structures combining the individualized, crosslinked fibers ofthe present invention and hydrogel-forming materials, according to theskin wetness level measured by an evaporimeter subsequent to contactingmoistened absorbent structures to human skin. This improvement isbelieved due to the high wicking ability of individualized, crosslinkedfibers relative to conventional fibers and the increased absorptivecapacity of the structure. Unique wicking ability of structures madefrom individualized, crosslinked fibers results from the stiff nature ofthe fibers and the relatively large void spaces resulting therefrom.However, excessively high levels of crosslinking agent, as may bepresent in certain prior known individualized, crosslinked fibers, mayreduce wicking due to the hydrophobic characteristics of thecrosslinking agent.

Another important advantage has been observed with respect to absorbentstructures made from individualized, crosslinked fibers having drydensities which are higher than their corresponding equilibrium wetdensities (calculated on a dry fiber basis). Specifically, this type ofabsorbent structure expands in volume upon wetting. As a result of thisexpansion, the interfiber capillary network of fibers also enlarges. Inconventional absorbent structures having hydrogel-forming materialblended therein, the hydrogel-forming material expands in volume due tofluid absorption, and may block or reduce in size the capillary routesfor fluid absorption prior to utilization of the entire fluid absorbingpotential of the structure. This phenomenon is known as gel blocking.Capillary enlargement due to expansion of fibrous network of theabsorbent structure reduces the occurrence of gel blocking. This allowslarger proportions of the fluid absorbency potential of the structure tobe utilized and allows higher levels of hydrogel-forming material (ifdesired) to be incorporated into the absorbent structure, withoutsignificant levels of gel-blocking.

Absorbent structures containing individualized, crosslinked fibers andhydrogel-forming material for diaper core applications preferably havedry densities of between about 0.15 g/cc and about 0.40 g/cc andpreferably contain less than about 20% hydrogel-forming material,calculated on a dry fiber weight basis. Most preferably, theindividualized, crosslinked fibers have between about 1.5 mole % andabout 6.0 mole % citric acid, calculated on a cellulose anhydroglucosemolar basis, reacted therewith in the form of intrafiber crosslink bondswherein the fibers are formed into a relatively thin absorbent structurein a sufficiently compressed dry state such that the structure mayexpand upon wetting.

The hydrogel-forming material may be homogeneously dispersed throughoutall or part of the absorbent structure. For a diaper structure asdisclosed in U.S. Pat. No. 3,860,003 having an absorbent core whichcontains the preferred individualized, crosslinked fibers, has a drydensity of about 0.20 g/cc, and also contains hydrogel-forming materialdispersed throughout the core. It is presently believed that an optimalbalance of diaper wicking, total absorbent capacity, skin wetness, andeconomic viability is obtained for contents of between about 5 wt. % andabout 20 wt. %, based on the total weight of the dry absorbent core, ofa hydrogen forming material such as Aqualic L-73. Between about 8 wt. %and about 10 wt. % of hydrogel-forming material is preferablyhomogeneously blended with the individualized, crosslinkedfiber-containing absorbent cores in products as disclosed in U.S. Pat.No. 3,860,003.

The absorbent structures described above may also include conventional,fluffed fibers, or highly refined fibers, wherein the amount ofhydrogel-forming material is based upon the total weight of the fibersas previously discussed. The embodiments disclosed herein are exemplaryin nature and are not meant to limit the scope of application ofhydrogel-forming materials with individualized, crosslinked fibers.

PROCEDURE FOR DETERMINING FLUID RETENTION VALUE

The following procedure can be utilized to determine the water retentionvalue of cellulosic fibers.

A sample of about 0.3 g to about 0.4 g of fibers is soaked in a coveredcontainer with about 100 ml distilled or deionized water at roomtemperature for between about 15 and about 20 hours. The soaked fibersare collected on a filter and transferred to an 80-mesh wire basketsupported about 11/2 inches above a 60-mesh screened bottom of acentrifuge tube. The tube is covered with a plastic cover and the sampleis centrifuged at a relative centrifuge force of 1500 to 1700 gravitiesfor 19 to 21 minutes. The centrifuged fibers are then removed from thebasket and weighed. The weighed fibers are dried to a constant weight at105° C. and reweighed. The water retention value is calculated asfollows: ##EQU1## where, W=wet weight of the centrifuged fibers;

D=dry weight of the fibers; and

W-D=weight of absorbed water.

PROCEDURE FOR DETERMINING DRIP CAPACITY

The following procedure can be utilized to determine drip capacity ofabsorbent cores. Drip capacity is utilized as a combined measure ofabsorbent capacity and absorbency rate of the cores.

A four inch by four inch absorbent pad weighing about 7.5 g is placed ona screen mesh. Synthetic urine is applied to the center of the pad at arate of 8 ml/s. The flow of synthetic urine is halted when the firstdrop of synthetic urine escapes from the bottom or sides of the pad. Thedrip capacity is calculated by the difference in mass of the pad priorto and subsequent to introduction of the synthetic urine divided by themass of the fibers, bone dry basis.

PROCEDURE FOR DETERMINING WET COMPRESSIBILITY

The following procedure can be utilized to determine wet compressibilityof absorbent structures. Wet compressibility is utilized as a measure ofresistance to wet compression, wet structural integrity and wetresilience of the absorbent cores.

A four inch by four inch square pad weighing about 7.5 g is prepared,its thickness measured and density calculated. The pad is loaded withsynthetic urine to ten times its dry weight or to its saturation point,whichever is less. A 0.1 PSI compressional load is applied to the pad.After about 60 seconds, during which time the pad equilibrates, thethickness of the pad is measured. The compressional load is thenincreased to 1.1 PSI, the pad is allowed to equilibrate, and thethickness is measured. The compressional load is then reduced to 0.1PSI, the pad allowed to equilibrate and the thickness is again measured.The densities are calculated for the pad at the original 0.1 PSI load,the 1.1 PSI load and the second 0.1 PSI load, referred to as 0.1 PSIR(PSI rebound) load. The void volume reported in cc/g, is then determinedfor each respective pressure load. The void volume is the reciprocal ofthe wet pad density minus the fiber volume (0.95 cc/g). The 0.1 PSI and1.1 PSI void volumes are useful indicators of resistance to wetcompression and wet structural integrity. Higher void volumes for acommon initial pad densities indicate greater resistance to wetcompression and greater wet structural integrity. The difference between0.1 PSI and 0.1 PSIR void volumes is useful for comparing wet resilienceof absorbent pads. A smaller difference between 0.1 PSI void volume and0.1 PSIR void volume, indicates higher wet resilience.

Also, the difference in caliper between the dry pad and the saturatedpad prior to compression is found to be a useful indicator of theresponsiveness to wetting of the pads.

PROCEDURE FOR DETERMINING DRY COMPRESSIBILITY

The following procedure can be utilized to determine dry compressibilityof absorbent cores. Dry compressibility is utilized as a measure of dryresilience of the cores.

A four inch by four inch square air laid pad having a mass of about 7.5g is prepared and compressed, in a dry state, by a hydraulic press to apressure of 5500 lbs/16 in². The pad is inverted and the pressing isrepeated. The thickness of the pad is measured before and after pressingwith a no-load caliper. Density before and after pressing is thencalculated as mass/(area X thickness). Larger differences betweendensity before and after pressing indicate lower dry resilience.

PROCEDURE FOR DETERMINING LEVEL OF C₂ -C₉ POLYCARBOXYLIC ACID REACTEDWITH CELLULOSIC FIBERS

There exist a variety of analytical methods suitable for determining thelevel of polycarboxylic acid crosslinked with cellulosic fibers. Anysuitable method can be used. For the purposes of determining the levelof preferred C₂ -C₉ polycarboxylic acid (e.g., citric acid, 1,2,3propane tricarboxylic acid, 1,2,3,4 butane tetracarboxylic acid andoxydisuccinic acid) which reacts to form intrafiber crosslink bonds withthe cellulosic component of the individualized, crosslinked fibers inthe examples of the present invention, the following procedure is used.First, a sample of the crosslinked fibers is washed with sufficient hotwater to remove any unreacted crosslinking chemicals or catalysts. Next,the fibers are dried to equilibrium moisture content. The carboxyl groupcontent of the individualized, crosslinked fibers is then determinedessentially in accordance with T.A.P.P.I. Method T 237 OS-77. Thecrosslinking level of the C₂ -C₉ polycarboxylic acid is then calculatedfrom the fiber's carboxyl group content by the following formula:##EQU2## Where C=carboxyl content of crosslinked fibers, meq/kg30=carboxyl content of uncrosslinked pulp fibers meq/kg

*162 g/mole=molecular weight of crosslinked pulp fibers (i.e., oneanhydroglucose unit)

The assumptions made in deriving the above formula are:

1. The molecular weight of the crosslinked fibers is equivalent to thatof uncrosslinked pulp, i.e., 162 g/mole (calculated on an celluloseanhydroglucose molar basis). 2. Two of citric acid's three carboxylgroups react with hydroxyl groups on the cellulose to form a crosslinkbond, thus leaving one carboxyl group free to be measured by thecarboxyl test.

3. Two of tricarballylic acid's (TCBA, also known as 1,2,3 propanetricarboxylic acid) three carboxyl groups react with two hydroxyl groupson the cellulose to form a crosslink bond, thus leaving one carboxylgroup free to be measured by the carboxyl test.

4. Three of 1,2,3,4 butane tetracarboxylic acid's (BTCA) four carboxylgroups react with hydroxyl groups on the cellulose to form a crosslinkbond, thus leaving one carboxyl group free to be measured by thecarboxyl test.

5. Three of oxydisuccinic acid's (ODS) four carboxyl groups react withhydroxyl groups on the cellulose to form crosslink bond, thus leavingone carboxyl group free to be measured by the carboxyl test.

6. Uncrosslinked pulp fibers have a carboxyl content of 30 meq/kg.

7. No new carboxyl groups are generated on the cellulose during thecrosslinking process.

PROCEDURE FOR DETERMINING TWIST COUNT

The following method can be used to determine the twist count of fibersanalyzed in this disclosure.

Dry fibers are placed on a slide coated with a thin film of immersionoil, and then covered with a cover slip. The effect of the immersion oilwas to render the fiber transparent without inducing swelling andthereby aid in identification of the twist nodes (described below). Wetfibers are placed on a slide by pouring a low consistency slurry of thefibers on the slide which is then covered with a cover slip. The waterrendered the fibers transparent so that twist node identification isfacilitated.

An image analyzer comprising a computer-controlled microscope, a videocamera, a video screen, and a computer loaded with QUIPS software,available from Cambridge Instruments Limited (Cambridge, England;Buffalo, NY), is used to determine twist count.

The total length of fibers within a particular area of the microscopeslide at 200X magnification is measured by the image analyzer. The twistnodes are identified and marked by an operator. This procedure iscontinued, measuring fiber length and marking twist nodes until 1270 mminches of total fiber length are analyzed. The number of twist nodes permillimeter is calculated from this data by dividing the total fiberlength into the total number of twist nodes marked.

PROCEDURE FOR DETERMINING CURL FACTOR

The following method can be utilized to measure fiber curl index.

Dry fibers are placed onto a microscope slide. A cover slip is placedover the fibers and glued in place at the edges. The actual length L_(A)and the maximum projected length L_(R) (equivalent to the length of thelongest side of a rectangle encompassing the fiber) are measuredutilizing an image analyzer comprising a software controlled microscope,video camera, video monitor, and computer. The software utilized is thesame as that described in the Twist Count Image Analysis Method sectionabove.

Once L_(A) and L_(R) are obtained, the curl factor is calculatedaccording to Equation (1) shown above. The curl factor for each sampleof fiber is calculated for at least 250 individual fibers and thenaveraged to determine the mean curl factor for the sample. Fibers havingL_(A) less than 0.25 mm are excluded from the calculation.

The following examples illustrate the practice of the present inventionbut are not intended to be limiting thereof.

EXAMPLE I

Individualized, crosslinked fibers used in the absorbent structures ofthe present invention are made by a dry crosslinking process utilizingcitric acid as the crosslinking agent. The procedure used to produce thecitric acid crosslinked fibers is as follows:

1. For each sample, 1,735 g of once dried, southern softwood kraft (SSK)pulp is provided. The fibers have a moisture content of about 7%(equivalent to 93% consistency).

2. A slurry is formed by adding fibers to an aqueous solution containingabout 2,942 g of citric acid and 410 ml of 50% sodium hydroxide solutionin 59,323 g of H₂ O. The fibers are soaked in the slurry for about 60minutes. This step is also referred to as "steeping". The steep pH isabout 3.0.

3. The fibers are then dewatered by centrifuging to a consistencyranging from about 40% to about 50%. the centrifuged slurry consistencyof this step combined with the carboxylic acid concentration in theslurry filtrate in step 2 set the amount of crosslinking agent presenton the fibers after centrifuging. In this example, about 6 weight % ofcitric acid, on a dry fiber cellulose anhydroglucose basis is present onthe fibers after the initial centrifuging. In practice, theconcentration of the crosslinking agent in the slurry filtrate iscalculated by assuming a targeted dewatering consistency and a desiredlevel of chemicals on the fibers.

4. Next, the dewatered fibers are defibrated using a Sprout-Waldron 12"disk refiner (model number 105-A) whose plates are set at a gap whichyields fibers substantially individualized but with a minimum amount offiber damage. As the individualized fibers exit the refiner, they areflash dried with hot air in two vertical tubes in order to provide fibertwist and curl. The fibers contain approximately 10% moisture uponexiting these tubes and are ready to be cured. If the moisture contentof the fibers is greater than about 10% upon exiting the flash dryingtubes, then the fibers are dried with ambient temperature air until themoisture content is about 10%.

5. The nearly dry fibers are then placed on trays and cured in anair-through drying oven for a length of time and at a temperature whichin practice depends on the amount of citric acid added, dryness of thefibers, etc. In this example, the samples are cured at a temperature ofabout 188° C. for a period of about 8 minutes. Crosslinking is completedduring the period in the oven.

6. The crosslinked, individualized fibers are placed on a mesh screenand rinsed with about 20° C. water, soaked at 1% consistency for one (1)hour in about 60° C. water, screened, rinsed with about 20° C. water fora second time, centrifuged to about 60% fiber consistency, and dried toan equilibrium moisture content of about 8% with ambient temperatureair.

The resulting individualized crosslinked cellulosic fibers have a WRV of37.6 and contain 3.8 mole % citric acid, calculated on a celluloseanhydroglucose molar basis, reacted with the fibers in the form ofintrafiber crosslink bonds.

The dried fibers are air laid to form absorbent pads. The pads arecompressed with a hydraulic press to a density of 0.20 g/cc. The padsare tested for absorbency, resiliency, and amount of citric acid reactedaccording to the procedures defined herein. Citric acid reacted isreported in mole % calculated on a dry fiber cellulose anhydroglucosebasis. The results are reported in Table 1 and are compared to anabsorbent pad made from conventional, uncrosslinked cellulosic fibers.

                                      TABLE 1                                     __________________________________________________________________________         Citric Acid                                                                              Drip Cap.                                                                           Wet Compressibility                                     Sample                                                                             (mole %)                                                                            WRV  @ 8 ml/s                                                                            (cc/g)                                                  #    Reacted                                                                             (%)  (g/g) 0.1 PSI                                                                            1.1 PSI                                                                            0.1 PSIR                                      __________________________________________________________________________    1    0     79.2 4.56  8.95 5.38 5.90                                          2    3.8   37.6 14.55 10.29                                                                              6.68 7.38                                          __________________________________________________________________________

As can be seen from Table 1, the absorbent pads containingindividualized, citric acid crosslinked fibers (i.e., Sample 2) havesignificantly higher drip capacities and wet compressibilities at 0.1PSI, 1.1 PSI and 0.1 PSIR relative to pads containing conventional,uncrosslinked fibers (i.e., Sample 1). In addition to having improvedresponsiveness to wetting relative to conventional uncrosslinked fibers,the absorbent pads containing citric acid crosslinked fibers can besafely utilized in the vicinity of human skin.

EXAMPLE II

The individualized, crosslinked fibers of Example I are air laid to formabsorbent pads, and compressed with a hydraulic press to a density of0.10 g/cc. The pads are subsequently tested for absorbency, resiliency,and structural integrity according to the previously outlined wetcompressibility procedure. The results are reported in Table 2.

                  TABLE 2                                                         ______________________________________                                                 Wet Compressibility                                                  Sample   (cc/g)                                                               #        0.1 PSI       1.1 PSI 0.1 PSIR                                       ______________________________________                                        1        10.68         6.04    6.46                                           2        11.87         7.67    8.48                                           ______________________________________                                    

As can be seen from Table 2, the absorbent pads--at a dry fiber densityof 0.10 g/cc--containing individualized, citric acid crosslinked fibers(i.e., Sample 2) have significantly higher wet compressibilities at 0.1PSI, 1.1 PSI, and 0.1 PSIR relative to pads containing conventional,uncrosslinked fibers (i.e., Sample 1). In addition to having improvedresponsiveness to wetting, the absorbent pads containing citric acidcrosslinked fibers can be safely utilized in the vicinity of human skin.

EXAMPLE III

Individualized crosslinked fibers used in the absorbent structures ofthe present invention are made by a dry crosslinking process utilizing1,2,3,4 butane tetracarboxylic acid (BTCA) as the crosslinking agent.The individualized crosslinked fibers are produced in accordance withthe hereinbefore described process of Example I with the followingmodifications: The slurry in step 2 of Example I contains 150 g of drypulp, 1186 g of H₂ O, 64 g of BTCA and 4 g of sodium hydroxide. In step5, the fibers are cured at a temperature of about 165° C. for a periodof about 60 minutes.

The resulting individualized crosslinked cellulosic fibers have a WRV of32.9 and contain 5.2 mole % 1,2,3,4 butane tetracarboxylic acid,calculated on a cellulose anhydroglucose molar basis, reacted with thefibers in the form of intrafiber crosslink bonds.

The dried fibers are air laid to form absorbent pads. The pads arecompressed with a hydraulic press to a density of 0.20 g/cc. The padsare tested for absorbency, resiliency, and amount of 1,2,3,4 butanetetracarboxylic acid (BTCA) reacted according to the procedures definedherein. BTCA reacted is reported in mole % calculated on a dry fibercellulose anhydroglucose basis. The results are reported in Table 3 andare compared to an absorbent pad made from conventional, uncrosslinkedcellulosic fibers.

                  TABLE 3                                                         ______________________________________                                        Sam- BTCA             Drip Cap.                                                                             Wet Compressibility                             ple  (mole %) WRV     @ 8 ml/s                                                                              (cc/g)                                          #    Reacted  (%)     (g/g)   0.1 PSI                                                                             1.1 PSI                                                                             0.1 PSIR                            ______________________________________                                        1    0        79.2    4.56    8.95  5.38  5.90                                3    5.2      32.9    13.43   9.58  6.30  7.05                                ______________________________________                                    

As can be seen from Table 3, the absorbent pads containingindividualized, BTCA crosslinked fibers (i.e., Sample 3) havesignificantly higher drip capacities and wet compressibilities at 0.1PSI, 1.1 PSI, and 0.1 PSIR relative to pads containing conventional,uncrosslinked fibers (i.e., Sample 1). In addition to having improvedresponsiveness to wetting, the absorbent pads containing BTCAcrosslinked fibers can be safely utilized in the vicinity of human skin.

EXAMPLE IV

The individualized, crosslinked fibers of Example III are air laid intoabsorbent pads, and compressed with a hydraulic press to a density of0.10 g/cc. The pads are subsequently tested for absorbency, resiliency,and structural integrity according to the previously outlined wetcompressibility procedure. The results are reported in Table 4.

                  TABLE 4                                                         ______________________________________                                                 Wet Compressibility                                                  Sample   (cc/g)                                                               #        0.1 PSI       1.1 PSI 0.1 PSIR                                       ______________________________________                                        1        10.68         6.04    6.46                                           3        11.71         7.52    8.53                                           ______________________________________                                    

As can be seen from Table 4, the absorbent pads--at a dry fiber densityof 0.10 g/cc--containing individualized, BTCA crosslinked fibers (i.e.,Sample 3) have significantly higher wet compressibilities at 0.1 PSI,1.1 PSI, and 0.1 PSIR relative to pads at the same density containingconventional, uncrosslinked fibers (i.e., Sample 1). In addition tohaving improved responsiveness to wetting, the absorbent pads containingBTCA crosslinked fibers can be safely utilized in the vicinity of humanskin.

In Examples III and IV, substantially similar results are obtained whenthe 1,2,3,4 butane tetracarboxylic acid (BTCA) crosslinking agent isreplaced in whole, or in part, by an equivalent amount of 1,2,3 propanetricarboxylic acid.

EXAMPLE V

Individualized crosslinked fibers used in the absorbent structures ofthe present invention are made by a dry crosslinking process utilizingoxydisuccinic acid (ODS) as the crosslinking agent. The individualizedcrosslinked fibers are produced in accordance with the hereinbeforedescribed process of Example I with the following modifications: Theslurry in step 2 of Example I contains 140 g of dry pulp, 985 g of H₂ O,40 g of sodium salt of ODS and 10 ml of 98% sulfuric acid.

The resulting individualized crosslinked cellulosic fibers have a WRV of44.3 and contain 3.6 mole % oxydisuccinic acid, calculated on acellulose anhydroglucose molar basis, reacted with the fibers in theform of intrafiber crosslink bonds.

The dried fibers are air laid to form absorbent pads. The pads arecompressed with a hydraulic press to a density of 0.20 g/cc. The padsare tested for absorbency, resiliency, and amount of oxydisuccinic acid(ODS) reacted according to the procedures defined herein. ODS reacted isreported in mole % calculated on a dry fiber cellulose anhydroglucosebasis. The results are reported in Table 5 and are compared to anabsorbent pad made from conventional, uncrosslinked cellulosic fibers.

                  TABLE 5                                                         ______________________________________                                        Sam- ODS              Drip Cap.                                                                             Wet Compressibility                             ple  (mole %) WRV     @ 8 ml/s                                                                              (cc/g)                                          #    Reacted  (%)     (g/g)   0.1 PSI                                                                             1.1 PSI                                                                             0.1 PSIR                            ______________________________________                                        1    0        79.2    4.56    8.95  5.38  5.90                                4    3.6      44.3    14.3    10.04 6.24  6.86                                ______________________________________                                    

As can be seen from Table 4, the absorbent pads containingindividualized, ODS crosslinked fibers (i.e., Sample 4) havesignificantly higher drip capacities and wet compressibilities at 0.1PSI, 1.1 PSI, and 0.1 PSIR relative to pads containing conventional,uncrosslinked fibers (i.e., Sample 1). In addition to having improvedresponsiveness to wetting, the absorbent pads containing ODS crosslinkedfibers can be safely utilized in the vicinity of human skin.

EXAMPLE VI

The individualized, crosslinked fibers of Example V are air laid intoabsorbent pads, and compressed with a hydraulic press to a density of0.10 g/cc. The pads are subsequently tested for absorbency, resiliency,and structural integrity according to the previously outlined wetcompressibility procedure. The results are reported in Table 6.

                  TABLE 6                                                         ______________________________________                                                 Wet Compressibility                                                  Sample   (cc/g)                                                               #        0.1 PSI       1.1 PSI 0.1 PSIR                                       ______________________________________                                        1        10.68         6.04    6.46                                           4        11.25         7.25    7.90                                           ______________________________________                                    

As can be seen from Table 6, the absorbent pads--at a dry fiber densityof 0.10 g/cc--containing individualized, crosslinked fibers (i.e.,Sample 4) have significantly higher wet compressibilities at 0.1 PSI,1.1 PSI, and 0.1 PSIR relative to pads at the same density containingconventional, uncrosslinked fibers (i.e., Sample 1). In addition tohaving improved responsiveness to wetting, the absorbent pads containingODS crosslinked fibers can be safely utilized in the vicinity of humanskin.

What is claimed is:
 1. An absorbent structure comprising individualized,crosslinked wood pulp cellulosic fibers having between about 0.5 mole %and about 10.0 mole % of a C₂ -C₉ polycarboxylic acid crosslinkingagent, calculated on a cellulose anhydroglucose molar basis, reactedwith said fibers in an intrafiber ester crosslink bond form, whereinsaid crosslinked fibers have a water retention value of from about 25 toabout 60, and wherein said C₂ -C₉ polycarboxylic acid crosslinking agentis selected from the group consisting of:(i) aliphatic and alicyclic C₂-C₉ polycarboxylic acids having at least three carboxyl groups permolecule; and (ii) aliphatic and alicyclic C₂ -C₉ polycarboxylic acidshaving two carboxyl groups per molecule and having a carbon-carbondouble bond located alpha, beta to one or both of the carboxyl groups,wherein one carboxyl group in said C₂ -C₉ polycarboxylic acidcrosslinking agent is separated from a second carboxyl group by eithertwo or three carbon atoms.
 2. The absorbent structure of claim 1 whereinsaid fibers have between about 1.5 mole % and about 6.0 mole %crosslinking agent, calculated on a cellulose anhydroglucose molarbasis, reacted therewith in the form of intrafiber ester crosslinkbonds.
 3. The absorbent structure of claim 1 wherein said crosslinkingagent is selected from the group consisting of citric acid, 1, 2, 3, 4butane tetracarboxylic acid, and 1, 2, 3 propane tricarboxylic acid. 4.The absorbent structure of claim 3 wherein said crosslinking agent iscitric acid.
 5. The absorbent structure of claim 2 wherein saidcrosslinking agent is selected from the group consisting of citric acid,1,2,3,4 butane tetracarboxylic acid, and 1,2,3 propane tricarboxylicacid.
 6. The absorbent structure of claim 5 wherein said crosslinkingagent is citric acid.
 7. The absorbent structure of claim 6 wherein saidwater retention value is between about 28 and about
 50. 8. The absorbentstructure of claim 1 wherein said crosslinking agent is selected fromthe group consisting of oxydisuccinic acid, tartrate monosuccinic acidhaving the formula ##STR3## and tartrate disuccinic acid having theformula ##STR4## .
 9. The absorbent structure of claim 8 wherein saidcrosslinking agent is oxydisuccinic acid.
 10. The absorbent structure ofclaim 8 wherein said fibers have between about 1.5 mole % and about 6.0mole % crosslinking agent, calculated on a cellulose anhydroglucosemolar basis, reacted therewith in the form of intrafiber crosslinkbonds.
 11. The absorbent structure of claim 10 wherein said waterretention value is between about 28 and about
 50. 12. The absorbentstructure of claim 1, 4, 7, or 8, having a dry density and anequilibrium wet density calculated on a dry fiber weight basis, said drydensity being greater than said equilibrium wet density.
 13. Theabsorbent structure of claim 1, 4 or 8 wherein said absorbent structurehas a dry density of less than about 0.60 g/cc.
 14. The absorbentstructure of claim 1, 4 or 8 wherein said absorbent structure has a drydensity of between about 0.05 g/cc and about 0.15 g/cc.
 15. Theabsorbent structure of claim 7 wherein said absorbent structure has adry fiber density of between about 0.12 g/cc and about 0.60 g/cc and anequilibrium wet density, calculated on a dry fiber basis, which is lessthan said actual dry fiber density.
 16. The absorbent structure of claim11 wherein said absorbent structure has a dry fiber density of betweenabout 0.12 g/cc and about 0.60 g/cc and an equilibrium wet density,calculated on a dry fiber basis, which is less than said actual dryfiber density.
 17. The absorbent structure of claim 1 wherein saidstructure comprises between about 70% and about 95% individualizedcrosslinked fibers, and between about 30% and about 5% uncrosslinkedcellulosic fibers.
 18. The absorbent structure of claim 1 furthercomprising a hydrogel-forming material disposed upon said fibers. 19.The absorbent structure of claim 1 further comprising a hydrogel-formingmaterial disposed within said absorbent structure.
 20. The absorbentstructure of claim 19 wherein said hydrogel-forming material issubstantially homogeneously blended throughout at least part of saidabsorbent structure.
 21. The absorbent structure of claim 19 whereinsaid hydrogel-form material is disposed upon a sheet, said sheet beingplaced against said fibers.
 22. The absorbent structure of claim 17further comprising a hydrogen-forming material disposed within saidabsorbent structure.
 23. A disposable absorbent article comprising atopsheet, a backsheet connected to said topsheet, and an absorbentstructure as recited in claim 1, 15, 16, 18, 19, or 22, disposed betweensaid topsheet and said backsheet.
 24. The absorbent structure of claim 1wherein said absorbent structure has a basis weight of less than about800 g/m², and a dry density of less than about 0.60 g/cc.
 25. Theabsorbent structure of claim 19 having a dry density and an equilibriumwet density, calculated on a dry fiber weight basis, said dry densitybeing greater than said equilibrium wet density.
 26. The absorbentstructure of claim 25 wherein said absorbent structure has a dry densityof between about 0.12 g/cc and about 0.60 g/cc.
 27. The absorbentstructure of claim 26 wherein said fibers have between about 1.5 mole %and about 6.0 mole % crosslinking agent, calculated on a celluloseanhydroglucose molar basis, the water retention value of said fibers isfrom about 28 to about 50, and wherein said crosslinking agent is citricacid.